Industry 4.0 – A Driver for Technology Innovation in Biotech

 

‌The toolbox of bioprocessing technologies available today offers choices for each unit operation in an end-to-end process. This toolbox includes stainless steel, single-use or continuous platforms that are commercially available from multiple suppliers and that are aligned to the outputs of commercially available production bioreactors both fed batch and/or perfusion. This equips the Process Development (PD) group with the opportunity to design new manufacturing processes selecting the most suitable technology for each unit operation to improve process efficiency and performance. Rather than go for a fully stainless steel or a fully single-use process a third option exists which is to mix up the technology platforms in a so-called hybrid approach.


The metaphor that we will describe aligns to a subway map where the passenger has multiple options to get from Station A to Station B and the route will be influenced by factors such as ease of connection, access with luggage, frequency of trains etc. It is the same thought processes that need to be considered when designing a new bioprocess. Factors such as scale of operation, operational flow rates, buffer storage, product stability etc. all will influence the selection of a specific unit operation in the downstream process.


The benefits of technology selection include improved facility utilization, optimized productivity, improved product quality all leading to enhanced patient safety, key drivers in the adoption of the practices underpinning Industry 4.0. As we progress along the journey we see that automation, control and data management are key aspects of future new hybrid bioprocesses. In-line or at-line analytics will support the drive to improve product quality and patient safety as well as overall facility throughput. There will be an increased use of virtual reality to design facility layout and optimize equipment usability and digital twins will be used to evaluate various hybrid production scenarios and create risk mitigation strategies.


In order to address the challenges faced as we move forward with the adoption of Industry 4.0 we have developed several new technologies and product platforms that supplement the existing toolboxes and are potential enablers for process improvement and optimization. These will be illustrated and demonstrate how it should be possible to develop process flows using the technology platforms best optimised for optimal productivity based on kg product produced per year per unit facility footprint. As new modalities such as gene therapeutics and exosomes progress further towards the clinic so these approaches to process design and development will become more and more standardized in order to enable products to get to market faster at the most appropriate cost.

Speaker

peter levison

Peter R. Levison

 

‌Executive Director Business Development 

Pall Biotech

In his current position within Pall Biotech, Peter Levison is responsible for developing strategic partnerships and collaborations within the Biotech community through the management of a network of Global Thought Leaders and collaborative partners. Working with key industrialists and academics around the world, Peter is actively looking for solutions to tomorrow’s challenges today. Previously he has held global product management leadership roles in batch and continuous downstream processing.

Industry 4.0 – A Driver for Technology Innovation in Biotech

icon image

Find Out More About Single-Pass TFF

Download the application note to read a case study on how to save up to 30% of cost of goods per batch.

더 Biotech 웨비나
Our webinars keep you informed on the latest products and technologies, current industry topics, the latest trends and a range of innovations and solutions to help continuously improve your processes.
December 2020
Servicios de Validación de Filtración y Single Use Technology

Biotech | Pall Corporation 웨비나 시리즈

¡Todo sobre los ensayos de validaciones para cumplir con los máximos estándares regulatorios!

Hablaremos sobre puntos cruciales de los servicios de validación, incluyendo:

1. Necesidad de validación

2. Cómo se realizan los ensayos de validación

3. Análisis de riesgo: re uso de filtros y toma de decisión en ensayos a realizar

4. Servicio de Validación Pall: documentación requerida para iniciar una cotización

¡No pierdas esta segunda oportunidad!

등록